68788-9892 Ondansetron Hydrochloride

Product NDC:

68788-9892

Brand Name:

Ondansetron Hydrochloride

Generic Name:

Ondansetron Hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: Ondansetron Hydrochloride

Strength: 8.0

Unit: mg/1

Packages:

Code: 68788-9892-01

Description: 10 TABLET, FILM COATED in 1 BOTTLE (68788-9892-1)

Effective Date: Feb. 14, 2012

Discontinued: Nov. 8, 2019

Code: 68788-9892-03

Description: 30 TABLET, FILM COATED in 1 BOTTLE (68788-9892-3)

Effective Date: Feb. 14, 2012

Discontinued: Nov. 8, 2019

SEER*Rx Category:

Ancillary Therapy

Major Class:

Antiemetic

Minor Class:

5HT3 Receptor Antagonist

Orphan Drug Designation:

Status:

No Longer Used

CanMED: NDC